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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Critical RiskFDA Drug
Medications & Supplements/Dietary Supplements

Vegetal Vigra Capsules Recalled for Sildenafil Contamination

Agency Publication Date: August 31, 2023
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Summary

APG SEVEN, INC. is recalling 120 bottles of Vegetal Vigra, a product marketed for male sexual enhancement. FDA laboratory analysis found that the 200mg capsules are tainted with sildenafil, which is the active ingredient in the prescription drug Viagra, making this an unapproved drug. The recalled 8-count bottles were distributed nationwide and are labeled as manufactured by Hand-shaking (Int'l) Corp. USA with an expiration date of January 31, 2025.

Risk

Sildenafil can interact with nitrates found in some prescription medications, such as nitroglycerin, and may lower blood pressure to dangerous or life-threatening levels. This pose a significant risk to consumers with diabetes, high blood pressure, high cholesterol, or heart disease who often take nitrates.

What You Should Do

  1. The recalled product is Vegetal Vigra (200mg capsules) sold in 8-count bottles with UPC 8931028556885 and an expiration date of 01/31/2025.
  2. If you have health concerns, contact your healthcare provider or pharmacist. Return any unused product to the place of purchase for a refund, throw it away, or contact APG SEVEN, INC for further instructions.
  3. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: Vegetal Vigra (200mg capsules, 8-count bottle)
Variants: 200mg capsules, 8-count bottle
UPC Codes:
8931028556885
Lot Numbers:
All lots (Exp 01/31/2025)

Manufacturer listed as Hand-shaking (Int'l) Corp. USA ADD: Hand-shaking Mansion, the 5th Ave., Stanford, USA.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 92892
Status: Active
Manufacturer: APG SEVEN, INC
Sold By: Retailers nationwide
Manufactured In: United States
Units Affected: 120 bottles
Distributed To: Nationwide
Agency Last Updated: September 15, 2023

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท FDA Press Release ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.